Home › Sickle Cell Disease › NCT07023666
Early Screening and Treatment of Heart Complication in Sickle Cell Disease
RecruitingPhase 2
Early Detection and Management of Cardiac Iron Overload in Sickle Cell Disease Using Multimodal Imaging for Improved Clinical Outcomes
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * At least 18 years of age * Diagnosis of sickle cell disease (any genotype) * Serum ferritin levels ≥ 400 ng/mL (up to 80 patients), or less than 400 ng/mL in those who have cardiac symptoms including shortness of breath and lower extremity edema (up to 20 patients) * Willingness to undergo regular imaging (echocardiograms, ECG, cardiac MRI) * ECOG performance status of 0-1 * Able to read, understand and provide written informed consent * Deemed appropriate for participation by the treating physician Exclusion Criteria: * Unable to schedule and required follow-up visits * Medical comorbidities including: * Known heart failure * Unstable angina * Uncontrolled dysrhythmias * Acute pulmonary embolism * Active infection or severe comorbid conditions that in the view of the investigator would limit participation * History of hypersensitivity or contraindication to chelation therapy * Severe renal or hepatic impairment * Pregnancy of breastfeeding
About the study
This study tests whether early heart screening and treatment for iron overload in subjects with sickle cell disease can prevent heart problems and reduce hospitalizations.
What is being tested
- Deferoxamine (drug)
- Deferasirox (drug)
- Deferiprone (drug)
- Echocardiography (device)
- Electrocardiogram (ECG) (device)
Sponsor: Inova Health Care Services · Participants: 100 · Started: Oct 7, 2025
Contact the study team
- Keary Jane't · Phone: 571-472-3173
- Elahe Mollapour · Phone: 571-472-0615
Official record on ClinicalTrials.gov — NCT07023666
Locations in the U.S.
| Virginia | Inova Schar Cancer, Fairfax Inova Health Care Service, Falls Church |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.